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rs63751056

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs63751056(-;-)
Make rs63751056(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403301
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751056
ebirs63751056
HLIrs63751056
Exacrs63751056
Varsomers63751056
Maprs63751056
PheGenIrs63751056
hapmaprs63751056
1000 genomesrs63751056
hgdprs63751056
ensemblrs63751056
gopubmedrs63751056
geneviewrs63751056
scholarrs63751056
googlers63751056
pharmgkbrs63751056
gwascentralrs63751056
openSNPrs63751056
23andMers63751056
23andMe allrs63751056
SNP Nexus

SNPshotrs63751056
SNPdbers63751056
MSV3drs63751056
GWAS Ctlgrs63751056
Max Magnitude0
ClinVar
Risk rs63751056(;)
Alt rs63751056(;)
Reference rs63751056(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630440delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076041.2,